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Journal of Neurology|September 24, 2022
The inherited cerebellar ataxias: an updateGiulia Coarelli, Thomas Wirth, Christine Tranchant, et al.Cerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia with sensory neuropathy (SCA25)Giovanni Stevanin, Emmanuel Broussolle, Nathalie Streichenberger, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 30, 2026
Quantifying Placebo Effects in Hereditary Ataxia Trials: A Meta-Analysis of Scale for the Assessment and Rating of Ataxia (SARA) Score ChangesEmilien Petit, Adonis Beaubois-Gandoin, Alexandra Durr, et al.Brain : a Journal of Neurology|January 30, 2026
Non-Huntington's disease chorea: an expanding universe with acquired causesFrancisco Cardoso, Débora Maia, Ricardo Maciel, et al.Developmental Medicine and Child Neurology|September 25, 2015
Relapsing encephalopathy with cerebellar ataxia related to an ATP1A3 mutationRodolphe Dard, Cyril Mignot, Alexandra Durr, et al.Brain : a Journal of Neurology|March 14, 2022
Antisense therapies in neurological diseasesJean-Baptiste Brunet de Courssou, Alexandra Durr, David Adams, et al.Annals of Clinical and Translational Neurology|August 27, 2019
Oral mobility reflects rate of progression in advanced Friedreich's ataxiaStéphanie Borel, Peggy Gatignol, Mustapha Smail, et al.Elife|May 13, 2021
Propensity for somatic expansion increases over the course of life in Huntington diseaseRadhia Kacher, François-Xavier Lejeune, Sandrine Noël, et al.Journal of Medical Genetics|January 15, 2017
A liminal stage after predictive testing for Huntington diseaseMarcela Gargiulo, Sophie Tezenas du Montcel, Marie France Jutras, et al.Sleep Medicine|May 3, 2015
Nocturnal agitation in Huntington disease is caused by arousal-related abnormal movements rather than by rapid eye movement sleep behavior disorderDulce Neutel, Maya Tchikviladzé, Perrine Charles, et al.Pageof 33